EP0784771B1 - High voltage ceramic igniter - Google Patents
High voltage ceramic igniter Download PDFInfo
- Publication number
- EP0784771B1 EP0784771B1 EP95935720A EP95935720A EP0784771B1 EP 0784771 B1 EP0784771 B1 EP 0784771B1 EP 95935720 A EP95935720 A EP 95935720A EP 95935720 A EP95935720 A EP 95935720A EP 0784771 B1 EP0784771 B1 EP 0784771B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- resistivity
- hot zone
- group
- zone composition
- mixtures
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23Q—IGNITION; EXTINGUISHING-DEVICES
- F23Q7/00—Incandescent ignition; Igniters using electrically-produced heat, e.g. lighters for cigarettes; Electrically-heated glowing plugs
- F23Q7/22—Details
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/56—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
- C04B35/565—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide
- C04B35/575—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide obtained by pressure sintering
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/56—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
- C04B35/565—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide
- C04B35/575—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide obtained by pressure sintering
- C04B35/5755—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide obtained by pressure sintering obtained by gas pressure sintering
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/58—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides
- C04B35/581—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on aluminium nitride
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/64—Burning or sintering processes
- C04B35/645—Pressure sintering
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/64—Burning or sintering processes
- C04B35/645—Pressure sintering
- C04B35/6455—Hot isostatic pressing
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3217—Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3817—Carbides
- C04B2235/3826—Silicon carbides
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3852—Nitrides, e.g. oxynitrides, carbonitrides, oxycarbonitrides, lithium nitride, magnesium nitride
- C04B2235/3865—Aluminium nitrides
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3852—Nitrides, e.g. oxynitrides, carbonitrides, oxycarbonitrides, lithium nitride, magnesium nitride
- C04B2235/3886—Refractory metal nitrides, e.g. vanadium nitride, tungsten nitride
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3891—Silicides, e.g. molybdenum disilicide, iron silicide
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/54—Particle size related information
- C04B2235/5418—Particle size related information expressed by the size of the particles or aggregates thereof
- C04B2235/5436—Particle size related information expressed by the size of the particles or aggregates thereof micrometer sized, i.e. from 1 to 100 micron
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/94—Products characterised by their shape
Definitions
- Ceramic materials have enjoyed great success as igniters in gas fired furnaces, stoves and clothes dryers. Ceramic igniter production requires constructing an electrical circuit through a ceramic component, a portion of which is highly resistive and rises in temperature when electrified by a wire lead.
- AlN aluminum nitride
- MoSi 2 molybdenum disilicide
- SiC silicon carbide
- the 24V Mini-IgniterTM when used in such applications, the 24V Mini-IgniterTM is subject to temperature runaway and so requires a transformer in the control system to step down from conventional line voltage (i.e., 120 volts). Accordingly, there is a need for small, higher voltage igniters designed for either 120 or 230 line voltage applications which do not require an expensive transformer but still possess the following requirements set by the appliance and heating industries to anticipate variation in line voltage: Time to design temperature ⁇ 5 sec Minimum temperature at 85% of design voltage 1100°C Design temperature at 100% of design voltage 1350°C Maximum temperature at 110% of design voltage 1500°C Hot-zone Length ⁇ 38 mm ( ⁇ 1.5") Power (W) 65-100.
- the amperage used for these high voltage applications will likely be comparable to that used in 24 volt applications (i.e., about 1.0 amp), the increased voltage will likely be realized by increasing the resistance of the igniter.
- the Mini-IgniterTM is comprised of one highly resistive material (AlN), one moderately resistive material (SiC), and one highly conductive material (MoSi 2 ), one obvious avenue for increasing the igniter's resistivity is to reduce its MoSi 2 and SiC contents while adding AlN.
- one trial composition containing about 76 volume percent ("v/o" or "vol%") AlN, 9 v/o MoSi 2 , and 15 v/o SiC) was found to be unsatisfactory in that it not only was slow to reach the design temperature (due to low MoSi 2 levels), it also possessed a significant negative temperature coefficient of resistivity ("NTCR”) and so was subject to temperature runaway above about only 1350°C.
- a NTCR means that as the temperature of the igniter increases, its resistance decreases. This decrease makes the igniter hotter than it would be if the resistance was constant. If the NTCR is too extreme, the igniter is slow and cool at 85% and unstable at 110% of the rated voltage. Indeed, such an igniter may exhibit runaway at less than the 110% rating, in which case the amperage and temperature continue to rise even at a constant voltage until failure (burnout) occurs. Rather, it is preferable for the igniters to possess a positive temperature coefficient of resistance (“PTCR”) or a moderate NTCR.
- PTCR positive temperature coefficient of resistance
- a ceramic having a PTCR increases in resistivity when its temperature is increased from 1000°C to 1400°C
- a ceramic having a moderate NTCR decreases in resistivity by less than 25% when its temperature is increased from 1000°C to 1400°C.
- Either a PTCR or a moderate NTCR would allow for a more gradual temperature increase with increasing voltage, which is critical for 120V applications because, as explained above, the igniter must operate stably over a broad range of voltage.
- a green body comprising:
- a ceramic igniter for heating, wherein a line voltage of between 120 V and 230 V is provided across a ceramic igniter having a hot zone composition comprising :
- Figure 1 presents a typical microstructure of the present invention wherein the AlN is gray, the SiC is light gray, the MoSi 2 is white, and (it is believed) the alumina/aluminum oxynitride mixture is dark gray.
- the igniter of the present invention possesses both the resistivity required for high voltage applications and the quick time to temperature required by the heating and appliance industries.
- the resistivity-enhancing compound is a mixture of alumina and aluminum oxynitride.
- This mixture may be produced merely by adding alumina to the green body.
- alumina reacts with a portion of the aluminum nitride to form a crystalline aluminum oxynitride phase.
- the presence of the aluminum oxynitride phase in the ceramic has been confirmed by x-ray diffraction analysis. Dissolution of impurities into this crystalline phase is believed to increase the refractoriness of the intergranular phase, resulting in a decrease in ionic conductivity through the intergranular phase with increasing temperature.
- the alumina addition is believed to increase grain growth, resulting in a portion of the conductive phase being isolated, thus increasing the resistivity.
- any conventional alumina powder may be selected. It is generally added to the green body as alumina grain in an amount between about 0.5 and 18.5 v/o, preferably between about 0.5 and 6.5 v/o, more preferably about 2.5 to 3.5 v/o.
- alumina powder having an average grain size of between about 0.1 and about 10 microns, and only about 0.2 w/o impurities, is used.
- the alumina has a grain size of between about 0.3 and about 10 um. More preferably, Alcoa A17 calcined alumina, available from Alcoa Industrial Chemicals of Bauxite, Arkansas, is used.
- alumina may be introduced in forms other than a powder, including, but not limited to, alumina sol-gel approaches and hydrolysis of a portion of the aluminum nitride to produce a green body having about 2-20 vol%, and preferably about 2-8 vol%, alumina.
- Examples I-III set out below each add only alumina to the conventional AlN-MoSi 2 -SiC system, it is contemplated that compounds such other metallic oxides, metallic oxynitrides, rare earth oxides (e.g., 5 v/o yttria), rare earth oxynitrides, and mixtures thereof, may be substituted for alumina in the green body of the present invention and desirable results would still be obtained.
- the hot zone composition should include(a) between about 50 and about 80 v/o of an electrically insulating ceramic having a resistivity of at least about 10 10 ohm-cm; (b) between about 10 and about 45 v/o of a semiconductive material having a resistivity of between about 1 and about 10 8 ohm-cm; (c) between about 5 and about 25 v/o of a metallic conductor having a resistivity of less than about 10 -2 ohm-cm; and (d) between about 2.0 and about 20 v/o of a resistivity-enhancing compound selected from the group consisting of metallic oxides, metallic oxynitrides, rare earth oxides, rare earth oxynitrides, and mixtures thereof.
- the hot zone comprises 50-70 v/o electrically insulating ceramic, 20-30 v/o of the semiconducting ceramic, 6-12 v/o of the conductive material, and 2-8 v/o of the resistivity-enhancing compound.
- an electrically insulating ceramic is a ceramic having a room temperature resistivity of at least about 10 10 ohm-cm. If the electrically insulating ceramic component is present as more than about 80 v/o of the hot zone composition (when the conductive ceramic is present at about 6 v/o), the resulting composition becomes too resistive and is insufficiently slow in achieving target temperatures at high voltages. Conversely, if it is present as less than about 50 v/o (when the conductive ceramic is present at about 6 v/o), the resulting ceramic becomes too conductive at high voltages.
- the hot zone is more conductive and the upper and lower bounds of the insulating fraction can be suitably raised to achieve the required voltage.
- the insulator is a nitride selected from the group consisting of aluminum nitride, silicon nitride and boron nitride.
- a semiconductive ceramic is a ceramic having a room temperature resistivity of between about 1 and 10 8 ohm-cm. If the semiconductive component is present as more than about 45 v/o of the hot zone composition (when the conductive ceramic is in the range of about 6-10 v/o), the resultant composition becomes too conductive for high voltage applications (due to lack of insulator). Conversely, if it is present as less than about 10 v/o (when the conductive ceramic is in the range of about 6-10 v/o), the resultant composition becomes too resistive (due to too much insulator).
- the semiconductor is a carbide selected from the group consisting of silicon carbide (doped and undoped), and boron carbide.
- a conductive material is one which has a room temperature resistivity of less than about 10 -2 ohm-cm. If the conductive component is present in an amount of more than about 25 v/o of the hot zone composition, the resultant ceramic becomes too conductive for high voltage applications, resulting in a unacceptably hot igniter. Conversely, if it is present as less than about 5 v/o, the resultant ceramic becomes too resistive for high voltage applications, resulting in an unacceptably cold igniter.
- the conductor is selected from the group consisting of molybdenum disilicide, tungsten disilicide, and nitrides such as titanium nitride, and carbides such as titanium carbide.
- the resistivity-enhancing compound is present in an amount of less than about 2.0 v/o of the hot zone composition, then its resistivity-enhancing effect is not significant. Conversely, if it is present in an amount of more than about 20 v/o, then the hot zone becomes too resistive for a speedy time to temperature in high voltage applications.
- it comprises between about 2-8 v/o of the hot zone composition, more preferably about 4-5 v/o.
- it is selected from the group consisting of metallic oxides, metallic oxynitrides, rare earth oxides, and rare earth oxynitrides.
- it is selected from the group consisting of aluminum oxynitride and alumina.
- the component fractions of aluminum nitride, molybdenum disilicide and silicon carbide disclosed in U.S. Patent No. 5,045,237 are used to construct the hot zone of the igniter of the present invention. It has been found that the AlN-SiC-MoSi 2 system is a flexible one which can produce igniters having resistivities ranging from about 0.001 to about 100 ohm-cm. Preferably, the particle sizes of both the starting powders and the grains in the sintered ceramic are similar to those described in the Washburn patent.
- the hot zone/cold zone igniter design as described in the Washburn patent may be suitably used in accordance with the present invention.
- the hot-zone provides the functional heating for gas ignition. It generally has a resistivity of at least about 0.04 ohm-cm, preferably at least about 0.2 ohm-cm in the temperature range of 1000 to 1600°C. Preferably, it comprises about 50 to 80 v/o aluminum nitride, and about 5-25 v/o MoSi 2 and 10-45 v/o SiC (in a volume ratio of about 1 part MoSi 2 to about 2 parts SiC), and about 2.0 to 20 v/o of the resistivity enhancing compound.
- the hot zone comprises about 60 v/o AlN, 11 v/o MoSi 2 , and 25 v/o SiC and 5.5 v/o aluminum oxynitride/alumina mixture.
- the average grain size (d 50 ) of the hot zone components in the densified body is as follows:
- the cold-zone allows for attachment of the wire leads.
- it also is comprised of AlN, SiC and MoSi 2 .
- it has a significantly higher percentage of the conductive and semiconductive materials (i.e., SiC and MoSi 2 ) than does the hot zone. Accordingly, it has typically only about 1/5 to 1/20 of the resistivity of the hot-zone composition and does not rise in temperature to the levels experienced by the hot zone.
- It preferably comprises about 20 to 65 v/o aluminum nitride, and about 20 to 70 v/o MoSi 2 and SiC in a volume ratio of from about 1:1 to about 1:3.
- the cold zone comprises about 60 v/o AlN, 20 v/o SiC and 20 v/o MoSi 2 . Because it does not require a high resistivity, the cold zone need not contain the aluminum oxynitride phase required by the hot zone of the present invention.
- the dimensions of the igniter affect its properties and performance.
- the single leg length of the hot zone should be greater than about 17,8 mm (0.700 inches) (to provide enough mass so that cooling convective gas flow will not significantly affect its temperature) but less than about 38,1 mm (1.500 inches) (to provide sufficient mechanical ruggedness).
- Its width should be greater than about 1,02 mm (0.04 inches) to provide sufficient strength and ease of manufacture.
- its thickness should be more than about 0,76 mm (0.03 inches) to provide sufficient strength and ease of manufacture.
- the two-legged hairpin igniters of the present invention are typically between about 31,8 and about 50,8 mm (1.25 and about 2.00 inches) in total single leg length, have a hot zone cross-section of between about 0.645 and 3,23 mm 2 (about 0.001 and about 0.005 square inches) (more preferably, less than 1,61 mm 2 (0.0025 square inches)).
- the hot zone is about 31,8 mm (1.25 inches) in single leg length, about 0,76 mm (0.03 inches) in thickness, and about 1,19 mm (0.047 inches) in width (i.e., a cross section of about 0,91 mm (0.00141 square inches)).
- Table I sets forth the dimensions of the hot zone of the igniter required for voltages using a hot zone composition of about 60 a/o AlN, about 11 v/o SiC, and about 25 v/o MoSi 2 , and about 4 v/o aluminum oxynitride/alumina mixture: Voltage Single Leg Length mm (in) Width mm (in) Thickness mm (in) 80 24,13 (about 0.95) 1,19 (0.047) 0,76 (0.030) 120 27,94 (about 1.10) 1,19 (0.047) 0,76 (0.030) 140 31,75 (about 1.25) 1,19 (0.047) 0,76 (0.030)
- the processing of the ceramic component i.e., green body processing and sintering conditions
- the preparation of the igniter from the densified ceramic can be done by any conventional method. Typically, such methods are carried out in substantial accordance with the Washburn patent. It has been found that higher sintering temperatures (i.e., above about 1800°C) tend to produce more grain growth in the aluminum nitride component of the igniter, resulting in a more isolated conductive component and therefore higher resistivity. However, it has been found that raising the sintering temperature above about 1820°C results in more igniter-to-igniter variability and lower fracture toughness.
- the key advantages of the igniter of the present invention are that it possesses a higher resistivity than the conventional small igniters and a moderate NTCR. It is believed that the moderate tendency towards temperature increase produced by the moderate NTCR of these igniters is comfortably balanced by the moderate tendency toward temperature decrease due to radiative heat loss, thereby leading to a self-controlling, temperature stable, high voltage igniter.
- 120V embodiments it has been found to be very insensitive to process variations, i.e., it is robust.
- Its hot zone resistance can be designed to be between about 100 and 300 ohms.
- Other properties of the 120V igniter of the present invention are comparable to those of the conventional 24 volt igniter.
- the igniters of the present invention have a power load per unit area of radiating surface of between about 25 and about 35 Watts/cm 2 a power consumption of between about 65-85 watts; a room temperature flexure strength of between about 400 and 500 MPa; and a resistivity of at least about 0.2 ohm-cm.
- the less extreme NTCR allows it to more stably operate within a high voltage regime and still attain the performance requirements of conventional igniters. Both the 120V and 230V embodiments achieve the performance criteria discussed above.
- a “stable" igniter is one which maintains a constant resistivity and a constant temperature at a given voltage.
- a hot zone composition comprising about 60 parts by volume AlN, about 11 parts by volume MoSi 2 , about 25 parts by volume SiC, and about 4 parts by volume Al 2 O 3 were blended in a high shear mixer.
- a cold-zone composition comprising about 20 parts by volume AlN, about 20 parts by volume MoSi 2 , and about 60 parts by volume SiC were similarly blended. These powder blends were then loaded into adjoining volumes of a hot press and hot pressed to form a billet of about 60% of theoretical density. This billet was then green machined in order to form two-zone tiles that were approximately 76,2 x 50,8 x 5,08 mm (3.00 x 2.00 x 0.20").
- the machined tiles were subjected to hot isostatic pressing in which the tiles were soaked at 1790 degrees C and 2,07 10 5 N/m 2 30,000 psi for 1 hour.
- the dense tile was diamond machined to a hairpin design igniter (i.e., 38,1 mm (1.5") single leg length x 0,76 mm (0.030”) thickness x 1,19 mm (0.047”) leg width with a 1,52 mm (0.060”) slot width.
- This igniter displayed good performance at 120V. It had a sufficiently high resistivity (0.3 ⁇ 0.05 ohm-cm at 1300°C), a low time-to-temperature (4 seconds to 1100°C), and was stable up to 132V.
- Igniters were prepared in a similar manner to that described in Example 1, except that the composition was 60 v/o AlN, 10 v/o MoSi 2 and 25 v/o SiC and 5 v/o alumina (Sumitomo AKP-30).
- This igniter displayed good performance at 230V. It had a sufficiently high resistivity (1.2 ohm-cm at 1300°C), a low time-to-temperature (5 seconds to 1100°C), and was stable up to 250V.
- Tiles prepared according to Comparative Example 2 were exposed to water with a temperature of 95°C for 20 minutes. After drying these tiles showed a weight gain of about 1% resulting from hydrolysis of the AlN which formed alumina upon heating to about 900°C. The tiles were then densified and igniters formed as described in Example 1.
- This igniter displayed good performance at 150V. It had a sufficient resistivity (0.4 ohm-cm at 1300°C), a low time to temperature (less than 5 seconds to 1100°C), and was stable up to about 180V.
- Igniters were prepared in a similar manner to that described in Example 1, except that the composition was 66-71 v/o AlN, 8.5-9 v/o MoSi 2 and 20.5-25 v/o SiC. There was no alumina used in this composition.
- this igniter In a 120V application, this igniter possessed a moderate time to temperature (6-7 seconds to 1100°C).
- Igniters were prepared in a similar manner to that described in Comparitive Example 1, except that the tiles were densified at a soak temperature of 1815°C.
- this igniter was not only slow (10 seconds to 1100°C), it was also unstable at 245V.
- Igniters were prepared in a similar manner to that described in Example 1, except that the composition was 65 v/o AlN, 10 v/o MoSi 2 and 25 v/o Sic. There was no alumina used in this composition.
- this igniter was found to have a resistivity of only about 0.1 ohm-cm, reaching 1300°C at only about 90V. It possessed this low resistivity even though it had less MoSi 2 than Example 1 and the same MoSi 2 concentration as Example 2.
- the igniters of the present invention may be used in many applications, including gas phase fuel ignition applications such as furnaces and cooking appliances, baseboard heaters, boilers and stove tops.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Organic Chemistry (AREA)
- Structural Engineering (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Ceramic Products (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Resistance Heating (AREA)
Description
| Time to design temperature | < 5 sec |
| Minimum temperature at 85% of design voltage | 1100°C |
| Design temperature at 100% of design voltage | 1350°C |
| Maximum temperature at 110% of design voltage | 1500°C |
| Hot-zone Length | < 38 mm (<1.5") |
| Power (W) | 65-100. |
characterized in that it additionally comprises
characterized in that the hot zone composition additionally comprises :
| Voltage | Single Leg Length mm (in) | Width mm (in) | Thickness mm (in) |
| 80 | 24,13 (about 0.95) | 1,19 (0.047) | 0,76 (0.030) |
| 120 | 27,94 (about 1.10) | 1,19 (0.047) | 0,76 (0.030) |
| 140 | 31,75 (about 1.25) | 1,19 (0.047) | 0,76 (0.030) |
Claims (24)
- A green body comprising :a) between 50 and 80 v/o of an electrically insulating ceramic grain having a resistivity of at least about 1010 ohm-cm ;b) between 10 and 45 v/o of a semiconductive ceramic grains having a resistivity of between about 1 and about 108 ohm-cm ;c) between, 5 and 25 v/o of a metallic conductor grains having a resistivity of less than about 10-2 ohm-cm ; characterized in that it additionally comprises :d) between 2.0 and 20 v/o of a resistivity -enhancing compound selected from the group consisting of metallic oxides, metallic oxynitrides, rare earth oxides, rare earth oxynitrides, and mixtures thereof.
- The green body of claim 1 characterized in that the resistivity enhancing compound is alumina.
- The green body of claim 2 characterized in that the electrically insulating ceramic is aluminum nitride and the alumina is present essentially as a coating on the aluminum nitride grains.
- The green body of claim 3 characterized in that the alumina is present as grains having an average grain size of between 2 and 10 microns, and comprises between 0,5 v/o and 18,5 v/o of said green body.
- A sintered ceramic having a hot zone composition comprising :a) between 50 and 80 vol% of an electrically insulating material consisting essentially of aluminum nitride ;b) between 10 and 45 vol% of a semiconductive material selected from the group consisting of boron carbide and silicon carbide, and mixtures thereof;c) between 5 and 25 vol% of a metallic conductor selected from the group consisting of molybdenum disilicide, tungsten disilicide and titanium nitride, and mixtures thereof ;
characterized in that the hot zone composition additionally comprisesd) between 0,5 and 18,5 vol% of a resistivity enhancing compound selected from the group consisting of aluminum oxide, aluminum oxynitride, and mixtures thereof, and present as grains having an average grain size of between about 2 and 10 microns. - A sintered ceramic having a hot zone composition comprising :a) between 50 and 80 vol% of an electrically insulating material consisting essentially of aluminum nitride ;b) between 10 and 45 vol% of a semiconductive material selected from the group consisting of boron carbide and silicon carbide, and mixtures thereof;c) between 5 and 25 vol% of a metallic conductor selected from the group consisting of molybdenum disilicide, tungsten disilicide, titanium nitride, and mixtures thereof ; and
characterized in that the hot zone composition additionally comprises :d) between 2 and 20 vol% of a resistivity enhancing compound selected from the group consisting of aluminum oxide, aluminum oxynitride, and mixtures thereof. - Use of a ceramic igniter, for heating, wherein a line voltage of between 120 V and 230 V is provided across the ceramic igniter having a hot zone composition comprising :a) between 50 and 80 v/o of an electrically insulating ceramic having a resistivity of at least about 1010 ohm-cm ;b) between 10 and 45 v/o of a semiconductive material having a resistivity of between about 1 and about 108 ohm-cm ;c) between 5 and 25 v/o of a metallic conductor having a resistivity of less than about 10-2 ohm-cm ;characterized in that the hot zone composition additionally comprises :d) between 2,0 and 20 v/o of a resistivity enhancing compound selected from the group consisting of metallic oxides, metallic oxynitrides, rare earth oxides, rare earth oxynitrides, and mixtures thereof.
- The use of claim 7 characterized that the electrically insulating ceramic is selected from the group consisting of aluminum nitride, silicon nitride and boron nitride.
- The use of claim 8 characterized that the semiconductive material is selected from the group consisting of silicon carbide and boron carbide.
- The use material of claim 9 characterized that the metallic conductor is selected from the group consisting of molybdenum disilicide, tungsten disilicide and titanium nitride.
- The use of claim 10 characterized that the electrically insulating ceramic is aluminum nitride.
- The use of claim 11 characterized that the semiconductive material is silicon carbide.
- The use of claim 12 characterized that the metallic conductor is molybdenum disilicide.
- The use of claim 13 characterized that the aluminum nitride comprises between 50 and 70 v/o of the hot zone composition.
- The use of claim 14 characterized that the silicon carbide comprises between 20 and 30 v/o of the hot zone composition.
- The use of claim 15 characterized that the molybdenum disilicide comprises between 6 and 12 v/o of the hot zone composition.
- The use of claim 16 characterized that the resistivity enhancing compound is selected from the group consisting of aluminum oxide, aluminum oxynitride, and mixtures thereof.
- The use of claim 10 characterized that the resistivity enhancing compound is selected from the group consisting of aluminum oxide, aluminum oxynitride, and mixtures thereof.
- The use of claim 18 characterized that the resistivity enhancing compound comprises between 2 and 8 v/o of the hot zone composition.
- The use of claim 18 characterized that the resistivity enhancing compound comprises about 4 v/o of the hot zone composition.
- The use of claim 18 characterized that the hot zone composition comprises between 0,5 to 18,5 v/o resistivity enhancing compound present as grains having an average grain size of between, 2 and 10 microns.
- The use of claim 17 characterized that the hot zone composition comprises between 0,5 to 6,5 v/o resistivity enhancing compound present as grains having an average grain size of between 2 and 10 microns.
- The use of claim 18 characterized that the line voltage is 120 V and the hot zone composition has a cross-section of less than 32,3 mm2 (0,050 sq.inches) and a single leg length of less than 38,1 mm (1,5 inches).
- The use of claim 18 characterized that the line voltage is 230 V, and the hot zone composition has a cross-section of less than 32,3 mm2 (0,050 sq. inches) and a single leg length of less than 38,1 mm (1,5 inches).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US319211 | 1981-11-09 | ||
| US08/319,211 US5514630A (en) | 1994-10-06 | 1994-10-06 | Composition for small ceramic igniters |
| PCT/US1995/012815 WO1996011361A1 (en) | 1994-10-06 | 1995-10-05 | High voltage ceramic igniter |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0784771A1 EP0784771A1 (en) | 1997-07-23 |
| EP0784771B1 true EP0784771B1 (en) | 2002-04-10 |
Family
ID=23241311
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP95935720A Expired - Lifetime EP0784771B1 (en) | 1994-10-06 | 1995-10-05 | High voltage ceramic igniter |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5514630A (en) |
| EP (1) | EP0784771B1 (en) |
| JP (1) | JPH10500766A (en) |
| KR (1) | KR100239834B1 (en) |
| CA (1) | CA2201627C (en) |
| DE (1) | DE69526359T2 (en) |
| DK (1) | DK0784771T3 (en) |
| MX (1) | MX9702537A (en) |
| WO (1) | WO1996011361A1 (en) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5820789A (en) * | 1995-10-05 | 1998-10-13 | Saint Gobain/Norton Industrail Ceramics Corp. | High voltage ceramic igniter |
| WO1997027432A1 (en) * | 1996-01-26 | 1997-07-31 | Saint-Gobain Industrial Ceramics, Inc. | Novel ceramic igniter and method of using the same |
| DE69706587T2 (en) * | 1996-03-29 | 2002-07-11 | Kabushiki Kaisha Toshiba, Kawasaki | Ceramic matrix composite and method of making the same |
| US5786565A (en) * | 1997-01-27 | 1998-07-28 | Saint-Gobain/Norton Industrial Ceramics Corporation | Match head ceramic igniter and method of using same |
| JP3983362B2 (en) * | 1997-12-10 | 2007-09-26 | 日本碍子株式会社 | Porous composite ceramics and method for producing the same |
| US6078028A (en) * | 1999-02-19 | 2000-06-20 | Saint-Gobain Industrial Ceramics, Inc. | Solderless ceramic igniter having a leadframe attachment |
| US6217312B1 (en) | 1999-04-29 | 2001-04-17 | General Electric Company | Ignition system for a gas appliance |
| US6168418B1 (en) | 1999-04-29 | 2001-01-02 | General Electric Company | Ignition system with delay switch for a gas appliance |
| AU2004237862B2 (en) * | 1999-12-20 | 2006-06-22 | Saint-Gobain Ceramics And Plastics, Inc. | Compositions for ceramic igniters |
| US6582629B1 (en) | 1999-12-20 | 2003-06-24 | Saint-Gobain Ceramics And Plastics, Inc. | Compositions for ceramic igniters |
| US6474492B2 (en) * | 2001-02-22 | 2002-11-05 | Saint-Gobain Ceramics And Plastics, Inc. | Multiple hot zone igniters |
| US6759624B2 (en) | 2002-05-07 | 2004-07-06 | Ananda H. Kumar | Method and apparatus for heating a semiconductor wafer plasma reactor vacuum chamber |
| AU2003232085A1 (en) * | 2002-05-09 | 2003-11-11 | Harmonics, Inc | Tapecast electro-conductive cermets for high temperature resistive heating systems |
| DE102006062374A1 (en) * | 2006-12-20 | 2008-06-26 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Ceramic electric heating element |
| EP2100525A1 (en) | 2008-03-14 | 2009-09-16 | Philip Morris Products S.A. | Electrically heated aerosol generating system and method |
| EP2110033A1 (en) | 2008-03-25 | 2009-10-21 | Philip Morris Products S.A. | Method for controlling the formation of smoke constituents in an electrical aerosol generating system |
| EP2110034A1 (en) | 2008-04-17 | 2009-10-21 | Philip Morris Products S.A. | An electrically heated smoking system |
| EP2113178A1 (en) | 2008-04-30 | 2009-11-04 | Philip Morris Products S.A. | An electrically heated smoking system having a liquid storage portion |
| EP2201850A1 (en) | 2008-12-24 | 2010-06-30 | Philip Morris Products S.A. | An article including identification information for use in an electrically heated smoking system |
| EP2253233A1 (en) | 2009-05-21 | 2010-11-24 | Philip Morris Products S.A. | An electrically heated smoking system |
| EP2319334A1 (en) * | 2009-10-27 | 2011-05-11 | Philip Morris Products S.A. | A smoking system having a liquid storage portion |
| EP2327318A1 (en) | 2009-11-27 | 2011-06-01 | Philip Morris Products S.A. | An electrically heated smoking system with internal or external heater |
| US9854839B2 (en) | 2012-01-31 | 2018-01-02 | Altria Client Services Llc | Electronic vaping device and method |
| PL2967145T3 (en) | 2013-03-15 | 2019-09-30 | Altria Client Services Llc | System and method of obtaining smoking topography data |
| KR102278193B1 (en) | 2013-05-21 | 2021-07-19 | 필립모리스 프로덕츠 에스.에이. | Electrically heated aerosol delivery system |
| HUE071643T2 (en) | 2013-12-03 | 2025-09-28 | Philip Morris Products Sa | Aerosol-generating article and electrically operated system incorporating a taggant |
| TWI697289B (en) | 2014-05-21 | 2020-07-01 | 瑞士商菲利浦莫里斯製品股份有限公司 | Aerosol-forming article, electrically heated aerosol-generating device and system and method of operating said system |
| KR102601832B1 (en) | 2014-12-16 | 2023-11-14 | 필립모리스 프로덕츠 에스.에이. | Tobacco sachet for use in a tobacco vaporiser |
| KR102628155B1 (en) | 2015-02-27 | 2024-01-23 | 필립모리스 프로덕츠 에스.에이. | Feedback-controlled RTD adjustment for aerosol-generating devices |
| EP3352594B1 (en) | 2015-09-24 | 2019-11-06 | Philip Morris Products S.a.s. | Aerosol-generating system with capacitor |
| WO2017051006A1 (en) | 2015-09-24 | 2017-03-30 | Philip Morris Products S.A. | Aerosol-generating device with electrodes for measuring an electrical load |
| US10939704B2 (en) | 2015-09-24 | 2021-03-09 | Philip Morris Products S.A. | Aerosol-generating article with capacitor |
| CN109068754A (en) | 2016-05-31 | 2018-12-21 | 菲利普莫里斯生产公司 | Product is generated with tubulose aerosol and the electrically operated aerosol of feature is kept to generate system |
| WO2017207442A1 (en) | 2016-05-31 | 2017-12-07 | Philip Morris Products S.A. | Electrically operated aerosol-generating system with means to detect a tubular aerosol-generating article |
| JP7162536B2 (en) | 2016-05-31 | 2022-10-28 | フィリップ・モーリス・プロダクツ・ソシエテ・アノニム | Electrically-operated aerosol-generating system with tubular aerosol-generating article having improved airflow |
| WO2017211600A1 (en) | 2016-06-08 | 2017-12-14 | Philip Morris Products S.A. | Electrically operated aerosol-generating system with multiple-component aerosol-generating article |
| CN109688850B (en) | 2016-09-14 | 2022-01-11 | 菲利普莫里斯生产公司 | Aerosol-generating system and method for controlling an aerosol-generating system |
| CN110785093B (en) | 2017-07-07 | 2023-04-07 | 菲利普莫里斯生产公司 | Aerosol-generating system with four contacts |
| KR20200143691A (en) | 2018-03-27 | 2020-12-24 | 에스씨피 홀딩스 언 어숨드 비지니스 네임 오브 나이트라이드 이그나이터스 엘엘씨 | High temperature surface igniter for cooktop |
| JP7627774B2 (en) | 2021-02-18 | 2025-02-06 | フィリップ・モーリス・プロダクツ・ソシエテ・アノニム | Aerosol generating device having a partition wall |
| EP4294219B1 (en) | 2021-02-18 | 2025-04-02 | Philip Morris Products S.A. | Replaceable cartridge for aerosol-generating device with slidable sealing element |
| US20240349789A1 (en) | 2021-09-01 | 2024-10-24 | Philip Morris Products S.A. | Aerosol-generating system with mouthpiece having sensorial media |
| KR20240053048A (en) | 2021-09-01 | 2024-04-23 | 필립모리스 프로덕츠 에스.에이. | Aerosol generating system with replaceable mouthpiece |
| KR20240046820A (en) | 2021-09-01 | 2024-04-09 | 필립모리스 프로덕츠 에스.에이. | Aerosol generating system mouthpiece with condensation management |
| EP4395574A2 (en) | 2021-09-01 | 2024-07-10 | Philip Morris Products S.A. | Mouthpiece with condensation management feature |
| KR20250019615A (en) | 2022-06-03 | 2025-02-10 | 필립모리스 프로덕츠 에스.에이. | Cartridge containing aerosol generating beads |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3895219A (en) * | 1973-11-23 | 1975-07-15 | Norton Co | Composite ceramic heating element |
| US3875476A (en) * | 1974-01-10 | 1975-04-01 | Honeywell Inc | Igniter element |
| US3875477A (en) * | 1974-04-23 | 1975-04-01 | Norton Co | Silicon carbide resistance igniter |
| CA1058673A (en) * | 1974-10-10 | 1979-07-17 | Frank J. Hierholzer (Jr.) | Silicon carbide shapes resistance heater elements |
| JPS5657284A (en) * | 1979-10-13 | 1981-05-19 | Ngk Spark Plug Co | Closed end porcelain ignition plug |
| US4486651A (en) * | 1982-01-27 | 1984-12-04 | Nippon Soken, Inc. | Ceramic heater |
| US5045237A (en) * | 1984-11-08 | 1991-09-03 | Norton Company | Refractory electrical device |
| CA1240710A (en) * | 1984-11-08 | 1988-08-16 | Malcolm E. Washburn | Refractory composition and products resulting therefrom |
| US5085804A (en) * | 1984-11-08 | 1992-02-04 | Norton Company | Refractory electrical device |
| US4626516A (en) * | 1985-07-31 | 1986-12-02 | General Electric Company | Infiltration of Mo-containing material with silicon |
| US5292691A (en) * | 1992-01-13 | 1994-03-08 | United Technologies Corporation | Molybdenum disilicide matrix composites reinforced with continuous ceramic fibers |
| US5292692A (en) * | 1992-01-13 | 1994-03-08 | United Technologies Corporation | Method for improving ceramic fiber reinforced molybdenum disilicide composites |
| US5191508A (en) * | 1992-05-18 | 1993-03-02 | Norton Company | Ceramic igniters and process for making same |
-
1994
- 1994-10-06 US US08/319,211 patent/US5514630A/en not_active Expired - Lifetime
-
1995
- 1995-10-05 DK DK95935720T patent/DK0784771T3/en active
- 1995-10-05 KR KR1019970702164A patent/KR100239834B1/en not_active Expired - Fee Related
- 1995-10-05 JP JP8512655A patent/JPH10500766A/en active Pending
- 1995-10-05 CA CA002201627A patent/CA2201627C/en not_active Expired - Fee Related
- 1995-10-05 EP EP95935720A patent/EP0784771B1/en not_active Expired - Lifetime
- 1995-10-05 WO PCT/US1995/012815 patent/WO1996011361A1/en not_active Ceased
- 1995-10-05 DE DE69526359T patent/DE69526359T2/en not_active Expired - Lifetime
- 1995-10-05 MX MX9702537A patent/MX9702537A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US5514630A (en) | 1996-05-07 |
| WO1996011361A1 (en) | 1996-04-18 |
| DE69526359D1 (en) | 2002-05-16 |
| KR100239834B1 (en) | 2000-01-15 |
| CA2201627C (en) | 2002-02-26 |
| KR970706474A (en) | 1997-11-03 |
| CA2201627A1 (en) | 1996-04-18 |
| EP0784771A1 (en) | 1997-07-23 |
| JPH10500766A (en) | 1998-01-20 |
| DE69526359T2 (en) | 2002-11-28 |
| DK0784771T3 (en) | 2002-08-05 |
| MX9702537A (en) | 1997-06-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5514630A (en) | Composition for small ceramic igniters | |
| MXPA97002537A (en) | Ceram high voltage lighter | |
| US4449039A (en) | Ceramic heater | |
| EP0956478B1 (en) | Match head ceramic igniter and method of using same | |
| JP2804393B2 (en) | Ceramic heater | |
| US5820789A (en) | High voltage ceramic igniter | |
| EP0335382B1 (en) | Electrically conductive ceramic material | |
| EP0876573B1 (en) | Novel ceramic igniter and method of using the same | |
| KR100421761B1 (en) | Novel ceramic igniter having improved oxidation resistance, and method of using same | |
| EP2648475A1 (en) | Ceramic heater element, ceramic heater, and glow plug | |
| US7195722B2 (en) | Compositions for ceramic igniters | |
| US6025579A (en) | Ceramic heater and method of manufacturing the same | |
| JPH1041052A (en) | Ceramic resistance heating element and method of manufacturing the same | |
| JPH01317170A (en) | Electrically conductive ceramic material | |
| JP2547423B2 (en) | Method for manufacturing conductive sialon | |
| JPH03152893A (en) | ceramic heater | |
| AU2004237862B2 (en) | Compositions for ceramic igniters | |
| JPH11288778A (en) | Resistive element | |
| JPH0610106B2 (en) | Variable conductivity ZrB2 composite sintered body | |
| JPH03152892A (en) | ceramic heater | |
| JPH11162619A (en) | Rapid temperature raising heater element | |
| JPH10284219A (en) | Ceramic heater |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| 17P | Request for examination filed |
Effective date: 19970506 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE DK FR GB IT NL |
|
| 17Q | First examination report despatched |
Effective date: 19980717 |
|
| RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: SAINT GOBAIN INDUSTRIAL CERAMICS, INC. |
|
| GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
| GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
| GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
| REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
| GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE DK FR GB IT NL |
|
| REF | Corresponds to: |
Ref document number: 69526359 Country of ref document: DE Date of ref document: 20020516 |
|
| RAP2 | Party data changed (patent owner data changed or rights of a patent transferred) |
Owner name: SAINT-GOBAIN CERAMICS AND PLASTICS, INC. |
|
| NLT2 | Nl: modifications (of names), taken from the european patent patent bulletin |
Owner name: SAINT-GOBAIN CERAMICS AND PLASTICS, INC. |
|
| REG | Reference to a national code |
Ref country code: DK Ref legal event code: T3 |
|
| ET | Fr: translation filed | ||
| PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
| 26N | No opposition filed |
Effective date: 20030113 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DK Payment date: 20061030 Year of fee payment: 12 |
|
| REG | Reference to a national code |
Ref country code: DK Ref legal event code: EBP |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DK Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20071031 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20091028 Year of fee payment: 15 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 20091024 Year of fee payment: 15 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IT Payment date: 20091028 Year of fee payment: 15 Ref country code: GB Payment date: 20091026 Year of fee payment: 15 Ref country code: FR Payment date: 20091029 Year of fee payment: 15 |
|
| REG | Reference to a national code |
Ref country code: NL Ref legal event code: V1 Effective date: 20110501 |
|
| GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20101005 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20101102 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20110630 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110501 Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20101005 |
|
| REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 69526359 Country of ref document: DE Effective date: 20110502 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20101005 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110502 |